Fuchs Gmbh & Co. KG
FDA import alert and refusal historyDissen am Teutoburger Wald, GermanyFEI 3004000145
As of October 26, 2026, Fuchs Gmbh & Co. KG (Dissen am Teutoburger Wald, Germany) is on the red list of FDA Import Alert 99-36 (Low-acid canned/acidified foods: process information) for amazon green peppercorns (whole) in brine, published by FDA on June 3, 2014, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-36 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Fuchs Gmbh & Co. KG
2 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-36red listAmazon green peppercorns (whole) in brineSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Fuchs Gmbh & Co. KG
- Is Fuchs Gmbh & Co. KG on an FDA import alert?
- Yes. As of October 26, 2026, Fuchs Gmbh & Co. KG is on the red list of FDA Import Alert 99-36, “Low-acid canned/acidified foods: process information”, for amazon green peppercorns (whole) in brine; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Fuchs Gmbh & Co. KG?
- No FDA import refusals for Fuchs Gmbh & Co. KG appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Fuchs Gmbh & Co. KG last inspected by FDA?
- FDA's most recent inspection of Fuchs Gmbh & Co. KG with a final classification is dated April 13, 2012 and was classified VAI (Voluntary Action Indicated).
- What is Fuchs Gmbh & Co. KG's FEI number?
- Fuchs Gmbh & Co. KG's FDA Establishment Identifier (FEI) is 3004000145.
- Can shipments from Fuchs Gmbh & Co. KG still enter the U.S.?
- Shipments of amazon green peppercorns (whole) in brine from Fuchs Gmbh & Co. KG can be detained without physical examination under Import Alert 99-36; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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